Tag | Content |
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EnhancerAtlas ID | HS026-02007 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr1:117013640-117015630 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr1:117015458-117015470 | CAAATCACTGCA | + | 7.22 | Hnf4a | MA0114.3 | chr1:117015191-117015207 | GAGGGCAAAGTCCTGT | + | 6.07 | Nkx2-5(var.2) | MA0503.1 | chr1:117015396-117015407 | CTTGAGTGCCT | - | 6.14 | RREB1 | MA0073.1 | chr1:117014694-117014714 | CCCCCCACCACCCCCCATCC | + | 7.75 | SPIC | MA0687.1 | chr1:117015285-117015299 | AAAAAGAGTAAGTA | + | 6.52 | Stat6 | MA0520.1 | chr1:117014435-117014450 | CCCTTCCTCAGAAGT | + | 6.01 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27848 | chr1:117013898-117021408 | Fetal_Intestine | SE_28774 | chr1:117013873-117021547 | Fetal_Intestine_Large | SE_50584 | chr1:117013866-117016332 | Sigmoid_Colon | SE_52493 | chr1:117013950-117016256 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I116471 | chr1 | 117014027 | 117021401 |
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Enhancer Sequence | TGAGAAATAA ATTTCTTTTT TTTTTTTAAA TAAATTACCC ACTCTGTGCT CTTCTGTTCT 60 AGCAACACAA AATGGACTAA GACACCATGG GCAGGGTCTC TGAGAAATAT GAGTTGAATA 120 GAAAAGTTTT CATCAAAATG CTGCTCAGTT GCTGAGGTAA AAGCCAACAG GGCTCAGACT 180 AGGGTGAGAT GAGTGAGACC AAGTCATACA AGTTACAGGA TCACATTTTG TCTTTATTTA 240 ACTTTTTTAG TGCATCATGA TTAATTGCAT TAATTTTTAT TTATTAAAAT ATCAATTATT 300 TTGATTGCTG AGTTTTTTCA CTCTGCCCCC ACAGCTCCCG GACCTGGGGG CCCCCACCCC 360 GTGAGCTCTG CCTTCCTGAT ACACAGATTA CAGGGGAAAC TCAGACTCCC TCTGCAGGAG 420 CTGGATGTCA GTTATCACCA GGGCTCAGCT GCGTATCCCG AGGGCTCACT CTGCTTGCCT 480 GATTCACCTC CCTTTCCAGT TTTGCCTTCC CTTCTTCCTC TAGCAGTCTG AGCATTCTGC 540 ACCTCCCCCT CCCTGTGCTT CAATGCCATC TCACCCAACA TCCACACTAG GGCTGCATGT 600 TCTCCAGAGC CTGCTCCATC CTTCCCTTCC CTTCTACCCA CAACTGACTT GCTTTATAAT 660 GGAAGAAGCG TTTTAATGCC TGCCATGAAA TCCTGTCATC TGGACAGGAA GGGCAAGCTC 720 CCTGGCTGAA TCATCAAGAG GAGAGCACCT GCCTGGAATA AGGCTCTGAA TCTTCTACAG 780 CTCTCTTTTC TGTTTCCCTT CCTCAGAAGT ATCCCCTGGA CACCGCAGAG GCTGTAGAAC 840 CAATACTGCC TGCACTGGCC AACTGTGGGG GCAGTGGCTT CACACCCCGT GTGTGCTGCA 900 AACACACTCA AATCTATGGC CTGTAATAAT TTCTGCACAT CCCTGTGTTG CTCCCATAGG 960 ACAGATAGAG GCACAAAGGC CCTGGCTGAT AAGTCGCATC AACTGATCAC ATAACCACTC 1020 ATTGACAAAA CAGAGATTAA ACCTATATTT TTGACCCCCC ACCACCCCCC ATCCTGTGTC 1080 CATTTCATTA TTCCATAAAC ATTCCCCTCT ACCACACCCT ACTTCCCCCT CACCTGCCCA 1140 CCCCTGCAAA GTCACTTGAT CTCTTGGTGA ATTAGCATGA GCCAACATTG ATGTTTTAAA 1200 ATAGCAAATT TTCAGGCTGA AAAAAGTCAA GATCATCTTT AAGTCCCCAA GGACATATGC 1260 AACCAGTGAT AGAAAAATCC TCTCCCACTT CTCCCCCTCC AGTCTGAATT GACTTAGCAA 1320 CTTTTCTTCA GCTCCTCAGC AGAGCCTTTC ACAAATTCCC ACTTGCAGCA CTGCTGAAGG 1380 ATAGACATCC TGATGTGCTC TCAGCTGGAC TGCTGCTGTG GGCTTCAAAA AAACAGATGC 1440 AGCAGCAGTG AGTGTGTGCC TGTATTATAT TTCTCAAGTG AACATCTTCA GAAGCTGGGG 1500 ACATGTGTTT TCTAGCCCAG CATGTAGGAT CTGTGGCCCC TGAGGCTGTG GGAGGGCAAA 1560 GTCCTGTAGA GAAGCTATTG TTTTCCTTGC CTTTGCTGAT AGCATGAGAT CAGCTAAATG 1620 ATGGTGGCAG GTATCCAAGA CCAAGAAAAA GAGTAAGTAG GGGTACAGTA ATGGGAAGCA 1680 GTAAATCGTA GGACATATTT GTAATCTAAG CAACAAAAAT CAAGCATTCT CTGGGAAATG 1740 CATGAAGCAC TGAATGCTTG AGTGCCTAAT GGGTTTTGAA GCCTCAGTAA GTTTATGTGG 1800 ATGGGTGCCA AGAGCAAACA AATCACTGCA GCCACAAGCT GCCTCACTCC ATATCCGAGA 1860 TGCATACTGA GAATGACTGG GAAGGCTACT TGGTATGGGA ACCCTAAAGC AGTTAGGATG 1920 GGGAGGCCCC CGGGGAAATG CTATCCTTAG TGCTCTCCAG GAAGCATCAT TTACAACTTC 1980 ACCATTGGCC 1990
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